ClinVar Miner

List of variants reported as uncertain significance for Mitochondrial complex 2 deficiency, nuclear type 4

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.113G>A (p.Arg38His)	rs143058777	0.00010
NM_003000.3(SDHB):c.304G>A (p.Ala102Thr)	rs777578399	0.00003
NM_003000.3(SDHB):c.749C>T (p.Thr250Ile)	rs1057517537	0.00001

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